Mutation

Primary Site >> Stomach Cancer

Gene >> MAP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694190:209694190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2020C>A
AA Mutation	p.His674Asn(p.H674N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209696664:209696664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4303A>G
AA Mutation	p.Arg1435Gly(p.R1435G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694483:209694483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2313A>C
AA Mutation	p.Lys771Asn(p.K771N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209710199:209710199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5018T>A
AA Mutation	p.Val1673Asp(p.V1673D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209693024:209693024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854C>A
AA Mutation	p.Ser285Tyr(p.S285Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695100:209695100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2930C>T
AA Mutation	p.Ala977Val(p.A977V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694576:209694576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2406G>T
AA Mutation	p.Met802Ile(p.M802I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695368:209695368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3198G>T
AA Mutation	p.Arg1066Ser(p.R1066S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209696551:209696551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4190G>T
AA Mutation	p.Arg1397Met(p.R1397M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209693400:209693400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780766647
CDS Mutation	c.1230A>C
AA Mutation	p.Glu410Asp(p.E410D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694879:209694879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2709A>C
AA Mutation	p.Lys903Asn(p.K903N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209710087:209710087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4906A>G
AA Mutation	p.Ile1636Val(p.I1636V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694321:209694321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2151C>G
AA Mutation	p.Asn717Lys(p.N717K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209705632:209705632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4637C>T
AA Mutation	p.Ser1546Phe(p.S1546F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209693315:209693315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1145C>G
AA Mutation	p.Ala382Gly(p.A382G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209693388:209693388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218A>C
AA Mutation	p.Lys406Asn(p.K406N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209696732:209696732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4371A>C
AA Mutation	p.Glu1457Asp(p.E1457D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209693216:209693216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046A>G
AA Mutation	p.Asp349Gly(p.D349G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695805:209695805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3635T>C
AA Mutation	p.Ile1212Thr(p.I1212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209696095:209696095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764541712
CDS Mutation	c.3925G>A
AA Mutation	p.Val1309Met(p.V1309M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209696237:209696237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754124367
CDS Mutation	c.4067G>T
AA Mutation	p.Arg1356Ile(p.R1356I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209710193:209710193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5012A>C
AA Mutation	p.Lys1671Thr(p.K1671T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694508:209694508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2338A>G
AA Mutation	p.Thr780Ala(p.T780A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694831:209694831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2661G>T
AA Mutation	p.Glu887Asp(p.E887D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695888:209695888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777899876
CDS Mutation	c.3718G>C
AA Mutation	p.Glu1240Gln(p.E1240Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209693614:209693614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444T>G
AA Mutation	p.Ser482Ala(p.S482A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209693370:209693370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1200A>C
AA Mutation	p.Glu400Asp(p.E400D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695922:209695922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142649637
CDS Mutation	c.3752G>A
AA Mutation	p.Arg1251His(p.R1251H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209730195:209730195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5282A>C
AA Mutation	p.Lys1761Thr(p.K1761T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209694701:209694701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372993675
CDS Mutation	c.2531G>A
AA Mutation	p.Arg844His(p.R844H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695385:209695385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576483648
CDS Mutation	c.3215T>G
AA Mutation	p.Leu1072Arg(p.L1072R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000360351
Start	209695114:209695114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2944G>C
AA Mutation	p.Glu982Gln(p.E982Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209694981:209694981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181175771
CDS Mutation	c.2811G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209694600:209694600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2430A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209692851:209692851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209696061:209696061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3891C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209730310:209730310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5397G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209696256:209696256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4086T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209695809:209695809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760894819
CDS Mutation	c.3639G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209694243:209694243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2073T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209692830:209692830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209695914:209695914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3744G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209693478:209693478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1308T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209710011:209710011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4830T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209653405:209653405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209710011:209710011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4830T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209653183:209653183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209695203:209695203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3033C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209692695:209692695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209695401:209695401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550587107
CDS Mutation	c.3231C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209692788:209692788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360351
Start	209694501:209694501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2331A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360351
Start	209696943:209696943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4420delA
AA Mutation	p.Thr1474GlnfsTer14(p.T1474Qfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	54
Mutation Consequence	stop_gained
Transcription ID	ENST00000360351
Start	209694883:209694883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2713C>T
AA Mutation	p.Arg905Ter(p.R905*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	55
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000360351
Start	209696653:209696654(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4292_4293insGTATATTTAACAAAATACAAAA
AA Mutation	p.Phe1431LeufsTer4(p.F1431Lfs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	56
Mutation Consequence	stop_gained
Transcription ID	ENST00000360351
Start	209705649:209705649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4654C>T
AA Mutation	p.Arg1552Ter(p.R1552*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	57
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360351
Start	209680803:209680804(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.432dupA
AA Mutation	p.Gln145ThrfsTer29(p.Q145Tfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	58
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360351
Start	209693111:209693112(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.943dupA
AA Mutation	p.Ser315LysfsTer18(p.S315Kfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	59
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360351
Start	209696942:209696943(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.4420dupA
AA Mutation	p.Thr1474AsnfsTer22(p.T1474Nfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	60
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360351
Start	209710077:209710078(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4898dupA
AA Mutation	p.Ser1634ValfsTer8(p.S1634Vfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript